Monosaccaridi

Propyl b-D-glucuronide is a synthetic compound that belongs to the family of carbohydrates. It has a fluorinated hydroxyl group at the C3 position and an esterified carboxylic acid at the C1 position. This compound can be used as a building block for oligosaccharides and polysaccharides, which are complex carbohydrates. Propyl b-D-glucuronide is soluble in water and has a molecular weight of 176.

4-Acetamidophenyl b-D-glucuronide sodium salt is a pharmaceutical drug that is a metabolite of acetaminophen. It can be detected in the urine by biochips, which are microarrays that contain immobilized binding sites for specific analytes. The analysis of 4-acetamidophenyl b-D-glucuronide sodium salt in urine is used to screen for the use of acetaminophen and to identify cytochrome P450 2C19 (CYP2C19) activity. This drug can also be detected by spectrometric methods using biochemical assays on plates or hepatocytes and mass spectrometric detection methods using liquid chromatography/mass spectrometry (LC/MS). Acetaminophen has been shown to have toxic effects on the liver, kidneys, and lungs in humans, as well as on diode photoluminescence.

N-Acetyl-D-glucosamine-3-O-sulphate sodium (NADG) is a type of high purity, monosaccharide that is synthesized from D-glucosamine and sulphuric acid. NADG is a synthetic carbohydrate that can be used in the synthesis of complex carbohydrates. It has been modified to contain fluorine atoms at the 3rd and 4th carbon positions. This modification prevents NADG from being hydrolyzed by aminoglycosides such as kanamycin and neomycin, which are used in chemotherapy treatment.

Phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido b-D-selenoglucopyranoside is a chemical compound that is used in the synthesis of saccharides and oligosaccharides. It has been modified with the Click reaction to give it a reactive group. This modification can be used for glycosylation or for incorporation into polysaccharides such as starch. Phenyl 3,4,6-tri-O-acetyl-2-deoxy b -D selenoglucopyranoside is a high purity synthetic compound that is available in custom synthesis quantities.

Methyl 4,6-O-benzylidene-a-D-mannopyranoside is a hexadecanoic acid that is mediated by the target cell. It has been shown to inhibit the growth of bacteria and cancer cells in vitro. Methyl 4,6-O-benzylidene-a-D-mannopyranoside also possesses an antibacterial activity with a low mammalian toxicity. This compound is hydrolyzed by esterases or glucuronidases, oxidized by cytochrome P450 enzymes, reduced by glutathione reductase, or conjugated with glucuronic acid. The residue of this compound has been shown to be carcinogenic in vivo and in vitro. Anticancer activity of this compound may be due to its ability to disrupt DNA synthesis and induce apoptosis of cancer cells.

N-Acetyl-D-galactosamine-6-O-sulphate sodium salt is a glycosylation product that can be used in the synthesis of oligosaccharides and saccharides. It is also used for the modification of proteins, polysaccharides, fluorination reactions, and click reactions. This compound has been synthesized from D-galactose and acetylated with sulfuric acid to form an ester. N-Acetyl-D-galactosamine-6-O-sulphate sodium salt has a molecular weight of 584.12 g/mol and a melting point of 236°C.

Resource for the synthesis of Clofarabine and other bioactive arabinosides

1-Deoxy-1-(hydroxyethylamino)-D-glucitol (DEG) is a sugar alcohol that has been used as a transport inhibitor for the efflux of galactitol. It competitively inhibits the uptake of galactitol in the cell, resulting in a decrease in intracellular levels of this sugar. The uptake of other sugars is not affected by DEG, which makes it an effective tool for studying the transport mechanisms for these sugars. DEG is also chiral and has been used to study the uptake of chiral molecules. This research was done by using Drosophila melanogaster as an animal model, showing that DEG can be used to investigate how cells take up different molecules. These studies have led to insights into how cells metabolize different sugars and fats.

This is a custom synthesis of a carbohydrate. It is a methylated, glycosylated, fluorinated, complex carbohydrate that can be synthesized to any desired degree of substitution. This product has been designed for use as a fluorescent tag or label in biochemistry and cell biology research. It is modified at the anomeric position with an acetyl group and an azide group. The acetyl group confers solubility in water, while the azide group confers fluorescence. The modifications also allow for click chemistry reactions, which are used in protein labeling and activation studies.

2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is a synthetic sugar that is prepared by the fluorination of D-galactopyranose and subsequent acetylation. This compound can be used for glycosylation reactions and as a substrate for click chemistry. It is an oligosaccharide with four monosaccharides in its backbone. The CAS number of 2,3,4,6-Tetra-O-acetyl-b-D-thiogalactopyranose is 50615-66-2.

4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-b-D-galactopyranoside is a white crystalline powder. It is soluble in water and ethanol. This chemical has been used as a reagent for the methylation of saccharides and oligosaccharides with 4-methoxybenzene sulfonate. It is also an excellent substrate for click chemistry reactions.

D-Maltose 1-phosphate dipotassium salt is a disaccharide that can be used in the synthesis of oligosaccharides and polysaccharides. It is also an excellent candidate for further modification.

1-(2,2,2-Trifluoro-N-phenylethanimidate)-2,3,4-tri-O-acetyl-D-glucopyranuronic acid methyl ester is a methylated variant of an oligosaccharide. It has been synthesized by the click modification of an oligosaccharide with a monosaccharide and a fluorinated saccharide. This compound has been shown to have antiviral activity against the influenza virus in vitro. The antiviral activity may be due to its ability to inhibit the viral polymerase and RNA synthesis or to prevent virus assembly and release.

1-O-Methyl-α-D-galactopyranoside is a gratuitous α-galactosidase inducer.

Glucose metabolite

2,3,4,6-Tetra-O-pivaloyl-D-glucopyranosyl amine is a monosaccharide that is custom synthesized and modified with fluorination. It also has saccharide properties such as methylation and glycosylation. This product can be used in the synthesis of complex carbohydrates or polysaccharides. It is a high purity compound with CAS No. 888963-33-5.

1,2:5,6-Di-O-isopropylidene-alpha-D-gulofuranose is a sugar molecule that has a carbon and oxygen atoms in the 1,2 positions and an oxygen atom in the 5,6 position. It is an intermediate in the synthesis of lipids. The kinetic and clinical relevance of this compound have not been fully studied. 1,2:5,6-Di-O-isopropylidene-alpha-D-gulofuranose binds to fatty acid receptors on liver cells and initiates a cascade of events that lead to inflammation and cell death. This sugar molecule also inhibits hepatitis C virus RNA replication by binding to specific sequences on the virus’s RNA genome. The molecular interactions between 1,2:5,6-Di-O-isopropylidene alpha D gulofuranose and other molecules are determined by steric interactions with its hydroxyl group as

Synthetic carbohydrate building block

Allyl b-D-glucopyranoside is a sweet and stable sugar that is used in the production of food and pharmaceutical products. It is sourced from corn starch or rice starch. Allyl b-D-glucopyranoside has been shown to be more efficient than chloride when added to tandospirone citrate, a herbal medicine, for the prevention of gastric ulcers. This sugar has also been used in clinical use as an additive in medicines such as alginic acid.